Betaprodine

Betaprodine

SCHEMBL394431

CCC(=O)O[C@]1(c2ccccc2)CCN(C)C[C@@H]1C.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Betaprodine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
DRD3 known ✓ P35462 2/20 0.67
OPRM1 known ✓ P35372 6/20 0.56
OPRD1 known ✓ P41143 5/20 0.56
OPRK1 known ✓ P41145 4/20 0.56
GAA known ✓ P10253 1/20 0.50
SLC6A4 known ✓ P31645 1/20 0.45
ADRA1A known ✓ P35348 1/20 0.45
KCNH2 known ✓ Q12809 1/20 0.45
LMNA P02545 1/20 1.00
NPSR1 Q6W5P4 1/20 0.62
KMT2A Q03164 2/20 0.54
MEN1 O00255 1/20 0.54
MAPK1 P28482 1/20 0.53
ALDH1A1 P00352 2/20 0.51
SLC22A1 O15245 1/20 0.45
MAPT P10636 1/20 0.43

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Alphaprodine SCHEMBL8818643 1.00 LMNA (1.00) LMNADRD3NPSR1OPRM1OPRD1
Betaprodine SCHEMBL186644 0.99 LMNA (0.97) LMNADRD3NPSR1OPRM1OPRD1
Betaprodine SCHEMBL248367 0.99 LMNA (0.97) LMNADRD3NPSR1OPRM1OPRD1
Alphaprodine SCHEMBL25054 0.99 LMNA (0.97) LMNADRD3NPSR1OPRM1OPRD1
Betaprodine SCHEMBL25053 0.99 LMNA (0.97) LMNADRD3NPSR1OPRM1OPRD1
Betaprodine SCHEMBL1649307 0.96 LMNA (0.93) LMNADRD3NPSR1OPRM1OPRD1
Proheptazine SCHEMBL25539 0.91 LMNA (0.84) LMNADRD3NPSR1OPRM1OPRD1
SCHEMBL11383571 0.88 LMNA (0.78) LMNADRD3NPSR1OPRM1OPRD1
Betaprodine SCHEMBL4283575 0.87 LMNA (0.77) LMNADRD3NPSR1OPRM1OPRD1
SCHEMBL8977860 0.87 LMNA (0.77) LMNADRD3NPSR1OPRM1OPRD1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 118 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0906104-A4 METHOD FOR TREATING PAIN LILLY CO ELI (US) 2003-12-10 EP claimed
US-20030013689-A1 Method for treating pain HELTON DAVID REED (US) 2003-01-16 US claimed
US-6444665-B1 USING AN ATYPICAL ANTIPSYCHOTIC COMPOUND TO PROVIDE ANALGESIC ACTIVITY; RISPERIDONE, CLOZAPINE, SEROQUEL, SERTINDOLE, ZIPRASIDONE, AND ZOTEPINE ELI LILLY AND COMPANY 2002-09-03 US claimed
JP-2000507544-A 2000-06-20 JP claimed
EP-0906104-A1 METHOD FOR TREATING PAIN ELI LILLY AND COMPANY (US) 1999-04-07 EP claimed
WO-1997035584-A1 METHOD FOR TREATING PAIN ELI LILLY AND COMPANY (US) 1997-10-02 WO claimed
US-11246873-B2 Directed differentiation of oligodendrocyte precursor cells to a myelinating cell fate THE SCRIPPS RESEARCH INSTITUTE (US) 2022-02-15 US disclosed
US-20200390780-A1 DIRECTED DIFFERENTIATION OF OLIGODENDROCYTE PRECURSOR CELLS TO A MYELINATING CELL FATE NOVARTIS INTERNATIONAL PHARMACEUTICAL LTD. (BM) 2020-12-17 US disclosed
US-10660899-B2 Directed differentiation of oligodendrocyte precursor cells to a myelinating cell fate THE SCRIPPS RESEARCH INSTITUTE (US) 2020-05-26 US disclosed
EP-2272508-B1 Pharmaceutical formulations for dry powder inhalers VECTURA LTD (GB) 2020-03-25 EP disclosed
US-10561613-B2 Method of making particles for use in a pharmaceutical composition VECTURA LIMITED (GB) 2020-02-18 US disclosed
EP-2266549-B1 METHOD OF MAKING PARTICLES FOR USE IN A PHARMACEUTICAL COMPOSITION VECTURA LTD (GB) 2019-08-07 EP disclosed
EP-1296651-B2 METHOD OF MAKING PARTICLES FOR USE IN A PHARMACEUTICAL COMPOSITION VECTURA LTD (GB) 2019-07-17 EP disclosed
EP-0906104-A1 METHOD FOR TREATING PAIN ELI LILLY AND COMPANY (US) 1999-04-07 EP disclosed
US-5891842-A CONCURRENT ADMINISTRATION OF AN OPIOD AND SUBSTANCE P OR PRECURSORS TRUSTEES OF TUFTS COLLEGE (US) 1999-04-06 US disclosed
WO-1997035584-A1 METHOD FOR TREATING PAIN ELI LILLY AND COMPANY (US) 1997-10-02 WO disclosed
US-4334526-A Method for administering a dissociative, unconscious type of anesthesia HAMACHER EDWARD N 1982-06-15 US disclosed
US-4334526-A Method for administering a dissociative, unconscious type of anesthesia HAMACHER EDWARD N 1982-06-15 US disclosed
US-4246894-A Method and system for administering a dissociative, unconscious type of anesthesia HAMACHER EDWARD N 1981-01-27 US disclosed
US-4246894-A Method and system for administering a dissociative, unconscious type of anesthesia HAMACHER EDWARD N 1981-01-27 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20030013689-A1 Method for treating pain OPRL1, OPRK1, ACHE DRD3 363/4885OPRM1 14/4885OPRD1 4/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.